Methods to Evaluate Changes in Mitochondrial Structure and Function in Cancer
Mitochondria are regulators of key cellular processes, including energy production and redox homeostasis. Mitochondrial dysfunction is associated with various human diseases, including cancer. Importantly, both structural and functional changes can alter mitochondrial function. Morphologic and quant...
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creator | Rickard, Brittany P Overchuk, Marta Chappell, Vesna A Kemal Ruhi, Mustafa Sinawang, Prima Dewi Nguyen Hoang, Tina Thuy Akin, Demir Demirci, Utkan Franco, Walfre Fenton, Suzanne E Santos, Janine H Rizvi, Imran |
description | Mitochondria are regulators of key cellular processes, including energy production and redox homeostasis. Mitochondrial dysfunction is associated with various human diseases, including cancer. Importantly, both structural and functional changes can alter mitochondrial function. Morphologic and quantifiable changes in mitochondria can affect their function and contribute to disease. Structural mitochondrial changes include alterations in cristae morphology, mitochondrial DNA integrity and quantity, and dynamics, such as fission and fusion. Functional parameters related to mitochondrial biology include the production of reactive oxygen species, bioenergetic capacity, calcium retention, and membrane potential. Although these parameters can occur independently of one another, changes in mitochondrial structure and function are often interrelated. Thus, evaluating changes in both mitochondrial structure and function is crucial to understanding the molecular events involved in disease onset and progression. This review focuses on the relationship between alterations in mitochondrial structure and function and cancer, with a particular emphasis on gynecologic malignancies. Selecting methods with tractable parameters may be critical to identifying and targeting mitochondria-related therapeutic options. Methods to measure changes in mitochondrial structure and function, with the associated benefits and limitations, are summarized. |
doi_str_mv | 10.3390/cancers15092564 |
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Mitochondrial dysfunction is associated with various human diseases, including cancer. Importantly, both structural and functional changes can alter mitochondrial function. Morphologic and quantifiable changes in mitochondria can affect their function and contribute to disease. Structural mitochondrial changes include alterations in cristae morphology, mitochondrial DNA integrity and quantity, and dynamics, such as fission and fusion. Functional parameters related to mitochondrial biology include the production of reactive oxygen species, bioenergetic capacity, calcium retention, and membrane potential. Although these parameters can occur independently of one another, changes in mitochondrial structure and function are often interrelated. Thus, evaluating changes in both mitochondrial structure and function is crucial to understanding the molecular events involved in disease onset and progression. This review focuses on the relationship between alterations in mitochondrial structure and function and cancer, with a particular emphasis on gynecologic malignancies. Selecting methods with tractable parameters may be critical to identifying and targeting mitochondria-related therapeutic options. Methods to measure changes in mitochondrial structure and function, with the associated benefits and limitations, are summarized.</description><identifier>ISSN: 2072-6694</identifier><identifier>EISSN: 2072-6694</identifier><identifier>DOI: 10.3390/cancers15092564</identifier><identifier>PMID: 37174030</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Adenosine triphosphate ; Bioenergetics ; Cancer ; Cancer therapies ; Cristae ; Cytology ; Development and progression ; Health aspects ; Homeostasis ; Localization ; Malignancy ; Membrane potential ; Metabolism ; Metabolites ; Metastases ; Metastasis ; Microscopy ; Mitochondria ; Mitochondrial DNA ; Morphology ; Oxidative stress ; Proteins ; Reactive oxygen species ; Respiration ; Review ; Structure-function relationships ; Therapeutic targets ; Visualization</subject><ispartof>Cancers, 2023-04, Vol.15 (9), p.2564</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). 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Mitochondrial dysfunction is associated with various human diseases, including cancer. Importantly, both structural and functional changes can alter mitochondrial function. Morphologic and quantifiable changes in mitochondria can affect their function and contribute to disease. Structural mitochondrial changes include alterations in cristae morphology, mitochondrial DNA integrity and quantity, and dynamics, such as fission and fusion. Functional parameters related to mitochondrial biology include the production of reactive oxygen species, bioenergetic capacity, calcium retention, and membrane potential. Although these parameters can occur independently of one another, changes in mitochondrial structure and function are often interrelated. Thus, evaluating changes in both mitochondrial structure and function is crucial to understanding the molecular events involved in disease onset and progression. This review focuses on the relationship between alterations in mitochondrial structure and function and cancer, with a particular emphasis on gynecologic malignancies. Selecting methods with tractable parameters may be critical to identifying and targeting mitochondria-related therapeutic options. Methods to measure changes in mitochondrial structure and function, with the associated benefits and limitations, are summarized.</description><subject>Adenosine triphosphate</subject><subject>Bioenergetics</subject><subject>Cancer</subject><subject>Cancer therapies</subject><subject>Cristae</subject><subject>Cytology</subject><subject>Development and progression</subject><subject>Health aspects</subject><subject>Homeostasis</subject><subject>Localization</subject><subject>Malignancy</subject><subject>Membrane potential</subject><subject>Metabolism</subject><subject>Metabolites</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Microscopy</subject><subject>Mitochondria</subject><subject>Mitochondrial DNA</subject><subject>Morphology</subject><subject>Oxidative stress</subject><subject>Proteins</subject><subject>Reactive oxygen species</subject><subject>Respiration</subject><subject>Review</subject><subject>Structure-function relationships</subject><subject>Therapeutic targets</subject><subject>Visualization</subject><issn>2072-6694</issn><issn>2072-6694</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNptkklPBCEQhYnRqFHP3kwnXryMsjRLn4yZuCVOPOidMHT1DKYHFGgT_720u0Y4UIHvPaiiENon-JixBp9Y4y3ERDhuKBf1GtqmWNKJEE29_iPeQnspPeAyGCNSyE20xSSRNWZ4G81mkJehTVUO1fmz6QeToZoujV9AqpyvZi4Huwy-jc701V2Og81DhMr4troYvM0u-JGbvr1lF210pk-w97HuoPuL8_vp1eTm9vJ6enYzsbVq8gSMbRjUIClXc2zmrZHcWKoU5tDKuhOW1KqTvC00VZxKLuaqs1ZywIR1bAedvts-DvMVtBZ8jqbXj9GtTHzRwTj9-8S7pV6EZ00wkVJgXhyOPhxieBogZb1yyULfGw9hSJoqwrgoBaMFPfyDPoQh-pLeSFGmqFD8m1qYHrTzXSgX29FUn8m6wY2gdKSO_6HKbGHlbPDQubL_S3DyLrAxpBSh-0qSYD02gf7TBEVx8LM2X_znl7NXuiOs3Q</recordid><startdate>20230429</startdate><enddate>20230429</enddate><creator>Rickard, Brittany P</creator><creator>Overchuk, Marta</creator><creator>Chappell, Vesna A</creator><creator>Kemal Ruhi, Mustafa</creator><creator>Sinawang, Prima Dewi</creator><creator>Nguyen Hoang, Tina Thuy</creator><creator>Akin, Demir</creator><creator>Demirci, Utkan</creator><creator>Franco, Walfre</creator><creator>Fenton, Suzanne E</creator><creator>Santos, Janine H</creator><creator>Rizvi, Imran</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7TO</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-6112-1290</orcidid><orcidid>https://orcid.org/0000-0001-9673-4700</orcidid><orcidid>https://orcid.org/0000-0003-0905-4083</orcidid><orcidid>https://orcid.org/0000-0003-3383-7782</orcidid><orcidid>https://orcid.org/0000-0002-8956-398X</orcidid><orcidid>https://orcid.org/0000-0001-8460-3260</orcidid><orcidid>https://orcid.org/0000-0001-6384-3070</orcidid></search><sort><creationdate>20230429</creationdate><title>Methods to Evaluate Changes in Mitochondrial Structure and Function in Cancer</title><author>Rickard, Brittany P ; 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subjects | Adenosine triphosphate Bioenergetics Cancer Cancer therapies Cristae Cytology Development and progression Health aspects Homeostasis Localization Malignancy Membrane potential Metabolism Metabolites Metastases Metastasis Microscopy Mitochondria Mitochondrial DNA Morphology Oxidative stress Proteins Reactive oxygen species Respiration Review Structure-function relationships Therapeutic targets Visualization |
title | Methods to Evaluate Changes in Mitochondrial Structure and Function in Cancer |
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